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Summary Literature (0)
DOID:0060682 - autosomal dominant nocturnal frontal lobe epilepsy 1

Disease Ontology Definition:An autosomal dominant nocturnal frontal lobe epilepsy that has_material_basis_in heterozygous mutation in the CHRNA4 gene on chromosome 20q13.

Synonyms: ENFL1, nocturnal frontal lobe epilepsy 1

Xenbase Genes : chrna4

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010899 - synchronous hermaphroditic organism

MIM:
MIM:600513 - EPILEPSY, NOCTURNAL FRONTAL LOBE, 1; ENFL1

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant nocturnal frontal lobe epilepsy (is_a)